Canonical Allele Identifier: CA1144879513
Gene: MTF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.37812783C= , CM000663.2:g.37812783C= GRCh38
NC_000001.10:g.38278455C= , CM000663.1:g.38278455C= GRCh37
NC_000001.9:g.38051042C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373036.5:c.*2353G= MANE Select ENSP00000362127.3:n.*2353G=
ENST00000373036.4:c.*2353G= ENSP00000362127.3:n.*2353G=
NM_005955.2:c.*2353G= NP_005946.2:n.*2353G=
XM_011541491.1:c.*2353G= XP_011539793.1:n.*2353G=
XM_011541492.1:c.*2353G= XP_011539794.1:n.*2353G=
XM_011541494.1:c.*2353G= XP_011539796.1:n.*2353G=
XM_011541491.2:c.*2353G= XP_011539793.1:n.*2353G=
NM_005955.3:c.*2353G= MANE Select NP_005946.2:n.*2353G=